Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Oticon A/S

US

Last updated May 24, 2026

What Oticon A/S makes

Oticon A/S manufactures a range of air-conduction hearing aids, including receiver-in-the-ear, behind-the-ear, in-the-ear, and canal models. Their portfolio also includes audiometric/hearing device software, wireless-fitting computer-aided systems, remote controls for hearing aids, and wireless induction loops for hearing aid users.

The company’s devices are classified under FDA categories Class I and Class II, with products listed in the FDA’s Unique Device Identifier (UDI) database. Oticon A/S is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Oticon A/S manufacture?

Oticon A/S specializes in air-conduction hearing aids, covering multiple form factors such as receiver-in-the-ear, behind-the-ear, in-the-ear, and canal models. Their portfolio also includes audiometric/hearing device software, wireless-fitting computer-aided systems, remote controls for hearing aids, and wireless induction loops designed to assist hearing aid users. These devices are developed to address various hearing loss needs and improve auditory access.

Where is Oticon A/S based, and does it operate internationally?

Oticon A/S is headquartered in the United States. While the company’s primary location is in the US, its devices are designed to meet global regulatory standards, including those in the FDA’s Unique Device Identifier (UDI) database. The company’s focus on hearing solutions suggests a broad market reach, though specific international operations or subsidiaries are not detailed in the available data.

Which regulatory registries list Oticon A/S’s devices?

Oticon A/S’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is used to track and identify medical devices in the United States, ensuring transparency and traceability for regulatory and market surveillance purposes. This listing applies to their air-conduction hearing aids and related accessories, as categorized under Class I and Class II devices.

How are Oticon A/S’s hearing aids classified by the FDA?

Oticon A/S’s hearing aids fall under two FDA device classes: Class I and Class II. Class I generally includes low-risk devices that pose minimal potential harm, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and benefits, as determined by regulatory authorities like the FDA.

What distinguishes Oticon A/S’s wireless-fitting computer-aided systems from other hearing aid technologies?

Oticon A/S’s wireless-fitting computer-aided systems are designed to streamline the customization and programming of hearing aids, enabling audiologists to adjust settings remotely and efficiently. These systems integrate with their air-conduction hearing aids to enhance fitting accuracy, user experience, and connectivity—such as pairing with smartphones or other devices—thereby improving accessibility and personalization for hearing aid users. This approach aligns with modern trends toward digital and wireless solutions in audiology.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
oticon.com
LinkedIn
—
Facebook
—
Phone
+4539177100
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
305839946

Catalogue (7693)

Page 104 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 109422
FDA UDI
Class IActive
Oticon 102-81-113-00
FDA UDI
Class IActive
Oticon 131666
FDA UDI
Class IIActive
Oticon 191897
FDA UDI
Class IIActive
Oticon 178956
FDA UDI
Class IIActive
Oticon 150074
FDA UDI
Class IIActive
Oticon 157436
FDA UDI
Class IIActive
Oticon 108989
FDA UDI
Class IIActive
Oticon 104-36-207-00
FDA UDI
Class IIActive
Oticon 214947
FDA UDI
Class IIActive
Oticon 204453
FDA UDI
Class IIActive
Oticon 191927
FDA UDI
Class IIActive
Hhm 133494
FDA UDI
Class IIActive
Hhm 151644
FDA UDI
Class IIActive
Oticon 150891
FDA UDI
Class IIActive
Agxo 103-37-062-00
FDA UDI
Class IIActive
Hhm 149226
FDA UDI
Class IIActive
Oticon 131909
FDA UDI
Class IIActive
Oticon 135326
FDA UDI
Class IActive
Oticon 196803
FDA UDI
Class IIActive
Oticon 207082
FDA UDI
Class IIActive
Oticon 196665
FDA UDI
Class IIActive
Hhm 148936
FDA UDI
Class IIActive
Oticon 118696
FDA UDI
Class IIActive
Oticon 103403
FDA UDI
Class IActive
Oticon 100701
FDA UDI
Class IIActive
Hhm 103-24-122-00
FDA UDI
Class IIActive
Oticon 106-29-240-10
FDA UDI
Class IIActive
Oticon 104-01-401-00
FDA UDI
Class IActive
Hhm 216059
FDA UDI
Class IIActive
Oticon 133776
FDA UDI
Class IIActive
Agxo 176107
FDA UDI
Class IIActive
Hhm 118710
FDA UDI
Class IIActive
Oticon 106-61-660-10
FDA UDI
Class IIActive
Oticon 196678
FDA UDI
Class IIActive
Oticon 131858
FDA UDI
Class IActive
Oticon 101549
FDA UDI
Class IIActive
Agxo 132306
FDA UDI
Class IIActive
Hhm 216010
FDA UDI
Class IIActive
EarQ 216244
FDA UDI
Class IIActive
Hhm 201749
FDA UDI
Class IIActive
Oticon 185783
FDA UDI
Class IIActive
Oticon 150754
FDA UDI
Class IIActive
Oticon 174005
FDA UDI
Class IIActive
Oticon 106-61-280-10
FDA UDI
Class IActive
Oticon 165425
FDA UDI
Class IIActive
Hhm 104-39-233-00
FDA UDI
Class IIActive
Oticon 209275
FDA UDI
Class IIActive
Hhm 126356
FDA UDI
Class IIActive
Oticon 191937
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.